Literature DB >> 713285

Hereditary polycystic kidney disease (adult form): a microdissection study of two cases at an early stage of the disease.

L Baert.   

Abstract

Kidney fragments from two cases of hereditary polycystic kidney disease (adult form) at an early stage were examined by microdissection. Localized cystic cystic dilatations were found in proximal and distal tubules, loops of Henle, and collecting tubules. Entirely normal nephrons and collecting tubules were also observed. Abnormal branching of collecting tubules or the abnormal attachment of nephrons, as described in other microdissection studies, were not found. Our observations do not confirm the hypothesis that the adult form of hereditary polycystic kidney disease is the consequence of ampullary dysfunction during early development.

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Year:  1978        PMID: 713285     DOI: 10.1038/ki.1978.75

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  32 in total

1.  Slowing Polycystic Kidney Disease by Fasting.

Authors:  Alessandra Boletta
Journal:  J Am Soc Nephrol       Date:  2015-11-04       Impact factor: 10.121

2.  The regulatory 1α subunit of protein kinase A modulates renal cystogenesis.

Authors:  Hong Ye; Xiaofang Wang; Megan M Constans; Caroline R Sussman; Fouad T Chebib; María V Irazabal; William F Young; Peter C Harris; Lawrence S Kirschner; Vicente E Torres
Journal:  Am J Physiol Renal Physiol       Date:  2017-06-14

Review 3.  Molecular advances in autosomal dominant polycystic kidney disease.

Authors:  Anna Rachel Gallagher; Gregory G Germino; Stefan Somlo
Journal:  Adv Chronic Kidney Dis       Date:  2010-03       Impact factor: 3.620

Review 4.  Why kidneys fail in autosomal dominant polycystic kidney disease.

Authors:  Jared J Grantham; Sumanth Mulamalla; Katherine I Swenson-Fields
Journal:  Nat Rev Nephrol       Date:  2011-08-23       Impact factor: 28.314

5.  Adult polycystic disease of the kidneys.

Authors: 
Journal:  Br Med J (Clin Res Ed)       Date:  1981-04-04

6.  In vitro function of cyst epithelium from human polycystic kidney.

Authors:  R D Perrone
Journal:  J Clin Invest       Date:  1985-10       Impact factor: 14.808

7.  Loss of polycystin-1 causes centrosome amplification and genomic instability.

Authors:  Lorenzo Battini; Salvador Macip; Elena Fedorova; Steven Dikman; Stefan Somlo; Cristina Montagna; G Luca Gusella
Journal:  Hum Mol Genet       Date:  2008-06-19       Impact factor: 6.150

8.  Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidney.

Authors:  C J Ward; H Turley; A C Ong; M Comley; S Biddolph; R Chetty; P J Ratcliffe; K Gattner; P C Harris
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-20       Impact factor: 11.205

9.  Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity.

Authors:  Katharina Hopp; Christopher J Ward; Cynthia J Hommerding; Samih H Nasr; Han-Fang Tuan; Vladimir G Gainullin; Sandro Rossetti; Vicente E Torres; Peter C Harris
Journal:  J Clin Invest       Date:  2012-10-15       Impact factor: 14.808

10.  Essential role of cleavage of Polycystin-1 at G protein-coupled receptor proteolytic site for kidney tubular structure.

Authors:  Shengqiang Yu; Karl Hackmann; Jiangang Gao; Jianggang Gao; Xiaobing He; Klaus Piontek; Miguel A García-González; Miguel A García González; Luis F Menezes; Hangxue Xu; Gregory G Germino; Jian Zuo; Feng Qian
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-14       Impact factor: 11.205

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